broadinstitute / gnomad-browserLinks
Explore gnomAD datasets on the web
☆85Updated this week
Alternatives and similar repositories for gnomad-browser
Users that are interested in gnomad-browser are comparing it to the libraries listed below
Sorting:
- ☆82Updated 7 years ago
- A modular annotation tool for genomic variants☆140Updated 2 weeks ago
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated last week
- ☆68Updated 2 weeks ago
- Hail helper functions for the gnomAD project and Translational Genomics Group☆98Updated last month
- IGV Web App☆126Updated 3 weeks ago
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆114Updated 6 years ago
- Workflows for converting between sequence data formats☆40Updated 4 years ago
- Genomic Interactive Visualization Engine☆146Updated 3 years ago
- This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are al…☆78Updated 5 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆163Updated 3 weeks ago
- MOsaic CHromosomal Alterations (MoChA) caller☆89Updated 4 months ago
- Documentation and description of AWS iGenomes S3 resource.☆119Updated last year
- Scalable gVCF merging and joint variant calling for population sequencing projects☆174Updated last year
- TransVar - multiway annotator for precision medicine☆126Updated 2 years ago
- ☆187Updated 2 years ago
- Somatic copy number analysis using WGS paired end wholegenome sequencing☆72Updated 5 years ago
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆158Updated 2 weeks ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated 2 weeks ago
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Updated 5 years ago
- Copy number calling and variant classification using targeted short read sequencing☆141Updated 4 months ago
- a Medical Genetics Sequence Analysis Pipeline☆84Updated last week
- HTML5 scrollable genome browser☆111Updated 2 years ago
- ☆69Updated 3 years ago
- A Python package for pharmacogenomics (PGx) research☆82Updated this week
- GA4GH Variation Representation Python Implementation☆61Updated this week
- Software program for checking sample matching for NGS data☆137Updated last year
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆91Updated 3 months ago